gabapentin
Generic: gabapentin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
gabapentin
Generic Name
gabapentin
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
gabapentin 800 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1041
Product ID
71335-1041_02a2ff55-579a-4049-a4f4-a9373b720d4e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203244
Listing Expiration
2026-12-31
Marketing Start
2014-01-11
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713351041
Hyphenated Format
71335-1041
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
gabapentin (source: ndc)
Generic Name
gabapentin (source: ndc)
Application Number
ANDA203244 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 800 mg/1
Packaging
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1041-1)
- 18 TABLET, FILM COATED in 1 BOTTLE (71335-1041-2)
- 58 TABLET, FILM COATED in 1 BOTTLE (71335-1041-3)
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1041-4)
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1041-5)
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-1041-6)
Packages (6)
71335-1041-1
90 TABLET, FILM COATED in 1 BOTTLE (71335-1041-1)
71335-1041-2
18 TABLET, FILM COATED in 1 BOTTLE (71335-1041-2)
71335-1041-3
58 TABLET, FILM COATED in 1 BOTTLE (71335-1041-3)
71335-1041-4
60 TABLET, FILM COATED in 1 BOTTLE (71335-1041-4)
71335-1041-5
30 TABLET, FILM COATED in 1 BOTTLE (71335-1041-5)
71335-1041-6
120 TABLET, FILM COATED in 1 BOTTLE (71335-1041-6)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "02a2ff55-579a-4049-a4f4-a9373b720d4e", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["b4954172-5439-48fd-8348-8a2e0d2fee62"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1041-1)", "package_ndc": "71335-1041-1", "marketing_start_date": "20190129"}, {"sample": false, "description": "18 TABLET, FILM COATED in 1 BOTTLE (71335-1041-2)", "package_ndc": "71335-1041-2", "marketing_start_date": "20240402"}, {"sample": false, "description": "58 TABLET, FILM COATED in 1 BOTTLE (71335-1041-3)", "package_ndc": "71335-1041-3", "marketing_start_date": "20240402"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1041-4)", "package_ndc": "71335-1041-4", "marketing_start_date": "20200428"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1041-5)", "package_ndc": "71335-1041-5", "marketing_start_date": "20190408"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-1041-6)", "package_ndc": "71335-1041-6", "marketing_start_date": "20181227"}], "brand_name": "Gabapentin", "product_id": "71335-1041_02a2ff55-579a-4049-a4f4-a9373b720d4e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71335-1041", "generic_name": "GABAPENTIN", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA203244", "marketing_category": "ANDA", "marketing_start_date": "20140111", "listing_expiration_date": "20261231"}